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首页> 外文期刊>Oncology reports >Phosphatase of regenerating liver-3 as a prognostic biomarker in histologically node-negative gastric cancer.
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Phosphatase of regenerating liver-3 as a prognostic biomarker in histologically node-negative gastric cancer.

机译:再生肝3的磷酸酶作为组织学阴性的胃癌的预后生物标志物。

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Phosphatase of regenerating liver-3 (PRL-3) has received attention as a molecule associated with metastasis in various tumor types, including gastric cancer. However, its clinical utility as a biomarker remains unclear in primary gastric cancer. The present study included 173 patients with primary gastric cancer who underwent gastrectomy with regional lymphadenectomy at the Kitasato University Hospital. All patients were informative for the well-characterized clinicopathological variables, including patient outcome. We assessed the potential as a clinically applicable biomarker using immunohistochemistry. PRL-3 overexpression was detected in 78 (45%) of 173 primary tumor tissues and was an independent predictor of lymph node metastasis on multivariate logistic regression analysis (odds ratio=9.32; P<0.0001). PRL-3 overexpression in primary tumor had significant prognostic implication (P=0.0009) and was also an independent prognostic factor (hazard ratio=4.39; P=0.006) in the histologically node-negative patients after curative resection, but not in the histologically node-positive patients. Moreover, in advanced gastric cancer with stage I disease, PRL-3 overexpression inversely affected patient outcome (P=0.02) and showed a characteristic of stage II disease from a prognostic point of view. We demonstrated for the first time that PRL-3 expression in primary tumor could predict the outcome of patients with histologically node-negative gastric cancer. We propose that PRL-3 expression can have a clinical potential as a prognostic biomarker that may facilitate the development of adjuvant chemotherapy for advanced gastric cancer with stage I disease.
机译:再生肝3(PRL-3)的磷酸酶作为一种与包括胃癌在内的各种肿瘤类型中的转移相关的分​​子受到关注。然而,在原发性胃癌中其作为生物标志物的临床用途尚不清楚。本研究包括在Kitasato大学医院接受胃切除和局部淋巴结清扫术的173例原发性胃癌患者。所有患者均了解特征明确的临床病理变量,包括患者预后。我们使用免疫组织化学评估了作为临床适用生物标志物的潜力。在173个原发性肿瘤组织中的78个(45%)中检测到PRL-3过表达,在多因素logistic回归分析中,PRL-3是淋巴结转移的独立预测因子(几率= 9.32; P <0.0001)。 PRL-3在原发肿瘤中的过表达具有显着的预后意义(P = 0.0009),并且在根治性切除后组织学淋巴结阴性的患者中也是一个独立的预后因素(危险比= 4.39; P = 0.006),但在组织学淋巴结中没有阳性患者。此外,在患有I期疾病的晚期胃癌中,PRL-3的过量表达反过来影响患者的预后(P = 0.02),并且从预后的角度显示II期疾病的特征。我们首次证明了PRL-3在原发性肿瘤中的表达可以预测组织学上呈阴性的胃癌患者的预后。我们建议PRL-3表达可作为临床预后生物标志物,可能有助于发展具有I期疾病的晚期胃癌辅助化疗的临床潜力。

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